Clorazepate Dipotassium 72789-0256
Product NDC
72789-0256- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- April 27, 2000
- Listing Expires
- December 31, 2026
- Application
- ANDA075731
Active Ingredients
| Ingredient | Strength |
|---|---|
| Clorazepate Dipotassium | 15 mg/1 |
Drug Class
Benzodiazepine [EPC]Benzodiazepines [CS]
Packaging Options(1)
6 TABLET in 1 BOTTLE, PLASTIC (72789-256-06)